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Transducer Cover

Vitrolife Sweden AB · Model 14201 · UDI-DI 17350025911646

HEM Prescription
1
510(k) clearances
1
Adverse events
1
Recalls
1
Facilities

Recalls

DateFirmReason
2008-05-12Digisonics, IncData/measurements from a OB report sent from ultrasound systems populated the wrong OB-View report

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.